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Annatto Tocotrienol Attenuates NLRP3 Inflammasome Activation in Macrophages

机译:安纳托生育三烯酚减弱巨噬细胞中的NLRP3炎性体激活。

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摘要

Accumulating evidence suggests that aberrant innate immunity is closely linked to metabolic diseases, including type 2 diabetes. In particular, activation of the NOD-like receptor family pyrin domain–containing 3 (NLRP3) inflammasome and subsequent secretion of interleukin 1β (IL-1β) are critical determinants that precipitate disease progression. The seeds of annatto (Bixa orellana L.) contain tocotrienols (T3s), mostly (>90%) in the δ form (δT3). The aim of this study was to determine whether annatto T3 is effective in attenuating NLRP3 inflammasome activation in macrophages. Our results showed that annatto δT3 significantly attenuated NLRP3 inflammasome by decreasing IL-1β reporter activity, IL-1β secretion, and caspase-1 cleavage against lipopolysaccharide (LPS) followed by nigericin stimulation. With regard to mechanism, annatto δT3 1) reduced LPS-mediated priming of the inflammasome and 2) dampened reactive oxygen species production, the second signal required for assembly of the NLRP3 inflammasome in macrophages. Our work suggests that annatto δT3 may hold therapeutic potential for delaying the onset of NLRP3 inflammasome–associated chronic metabolic diseases.
机译:越来越多的证据表明,先天免疫异常与包括2型糖尿病在内的代谢疾病密切相关。特别是,激活包含NOD的受体家族含3个pyrin结构域的炎性小体(NLRP3)和随后分泌白介素1β(IL-1β)是促成疾病进展的关键决定因素。 annatto(Bixa orellana L.)的种子含有生育三烯酚(T3s),其中大多数(> 90%)为δ形式(δT3)。这项研究的目的是确定annatto T3是否有效减弱巨噬细胞中的NLRP3炎性体激活。我们的结果表明,通过降低IL-1β的报道分子活性,IL-1β的分泌和对脂多糖(LPS)的caspase-1的裂解,随后降低黑素菌素的刺激,annattoδT3可以显着减轻NLRP3炎性体。就机理而言,annattoδT31)减少了LPS介导的炎性小体引发,2)抑制了活性氧的产生,这是在巨噬细胞中组装NLRP3炎性小体所需的第二个信号。我们的工作表明,annattoδT3可能具有延缓NLRP3炎性体相关慢性代谢疾病发作的治疗潜力。

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